Num | GeneID | Chromosome | Position | Ref.allele | Alt.allele | Mutant type | Impacts | Amino acid change | SampleID |
---|---|---|---|---|---|---|---|---|---|
1 | BAA05g01050 | A05 | 606838 | G | A | missense_variant | MODERATE | c.397C>T|p.Leu133Phe |
S238 |
2 | BAA05g01050 | A05 | 607118 | G | A | synonymous_variant | LOW | c.117C>T|p.Ser39Ser |
S241 |
3 | BAA05g01050 | A05 | 608307 | G | A | upstream_gene_variant | MODIFIER | c.-1073C>T| |
S153 |
4 | BAA05g01050 | A05 | 608555 | G | A | upstream_gene_variant | MODIFIER | c.-1321C>T| |
S233 |
5 | BAA05g01050 | A05 | 609049 | G | A | upstream_gene_variant | MODIFIER | c.-1815C>T| |
S46 |
6 | BAA05g01050 | A05 | 609957 | G | A | upstream_gene_variant | MODIFIER | c.-2723C>T| |
S273 |
7 | BAA05g01050 | A05 | 610625 | C | T | upstream_gene_variant | MODIFIER | c.-3391G>A| |
S167 |